scholarly article | Q13442814 |
P50 | author | Nobuyuki Uozumi | Q67904079 |
P2093 | author name string | Shunya Saito | |
P2860 | cites work | Role of stomata in plant innate immunity and foliar bacterial diseases | Q24654608 |
Predicting N-terminal myristoylation sites in plant proteins | Q24801683 | ||
Nitric oxide in guard cells as an important secondary messenger during stomatal closure | Q26823415 | ||
Sulfate transporters in the plant's response to drought and salinity: regulation and possible functions | Q26859143 | ||
Control of stomatal aperture: a renaissance of the old guard | Q27011653 | ||
There's more to the picture than meets the eye: nitric oxide cross talk with Ca2+ signaling | Q27011719 | ||
Homologue structure of the SLAC1 anion channel for closing stomata in leaves | Q27665402 | ||
Molecular basis of nitrate uptake by the plant nitrate transporter NRT1.1 | Q27681921 | ||
Structural basis for flg22-induced activation of the Arabidopsis FLS2-BAK1 immune complex | Q27687093 | ||
A Dominant Mutation in the HT1 Kinase Uncovers Roles of MAP Kinases and GHR1 in CO2-Induced Stomatal Closure. | Q39331107 | ||
Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells | Q39346722 | ||
Plant nitrogen nutrition: sensing and signaling | Q39373706 | ||
Biology of SLAC1-type anion channels - from nutrient uptake to stomatal closure | Q39443737 | ||
S-type Anion Channels SLAC1 and SLAH3 Function as Essential Negative Regulators of Inward K+ Channels and Stomatal Opening in Arabidopsis | Q39624990 | ||
NADPH oxidase AtrbohD and AtrbohF genes function in ROS-dependent ABA signaling in Arabidopsis. | Q39758932 | ||
Reconstitution of CO2 Regulation of SLAC1 Anion Channel and Function of CO2-Permeable PIP2;1 Aquaporin as CARBONIC ANHYDRASE4 Interactor | Q40110432 | ||
The Dual Role of Nitric Oxide in Guard Cells: Promoting and Attenuating the ABA and Phospholipid-Derived Signals Leading to the Stomatal Closure | Q40144083 | ||
Mechanisms of nitric-oxide-induced increase of free cytosolic Ca2+ concentration in Nicotiana plumbaginifolia cells | Q40288912 | ||
Guard cell SLAC1-type anion channels mediate flagellin-induced stomatal closure | Q40988102 | ||
Ca2+ and nucleotide dependent regulation of voltage dependent anion channels in the plasma membrane of guard cells | Q41233077 | ||
The role of malate in plant homeostasis | Q41811017 | ||
PYR/PYL/RCAR family members are major in-vivo ABI1 protein phosphatase 2C-interacting proteins in Arabidopsis | Q41988862 | ||
Open Stomata 1 (OST1) is limiting in abscisic acid responses of Arabidopsis guard cells | Q42444727 | ||
ATP binding to the C terminus of the Arabidopsis thaliana nitrate/proton antiporter, AtCLCa, regulates nitrate transport into plant vacuoles | Q42681081 | ||
The Arabidopsis vacuolar anion transporter, AtCLCc, is involved in the regulation of stomatal movements and contributes to salt tolerance. | Q42915051 | ||
Role of nitric oxide in regulating stomatal apertures. | Q43135725 | ||
Ozone-triggered rapid stomatal response involves the production of reactive oxygen species, and is controlled by SLAC1 and OST1. | Q43175417 | ||
Analysis of Arabidopsis with highly reduced levels of malate and fumarate sheds light on the role of these organic acids as storage carbon molecules. | Q43182569 | ||
Threonine at position 306 of the KAT1 potassium channel is essential for channel activity and is a target site for ABA-activated SnRK2/OST1/SnRK2.6 protein kinase | Q43270272 | ||
Phosphorylation of the Arabidopsis AtrbohF NADPH oxidase by OST1 protein kinase. | Q43283751 | ||
Phospholipase dalpha1 and phosphatidic acid regulate NADPH oxidase activity and production of reactive oxygen species in ABA-mediated stomatal closure in Arabidopsis. | Q43290048 | ||
ABA-Induced Stomatal Closure Involves ALMT4, a Phosphorylation-Dependent Vacuolar Anion Channel of Arabidopsis. | Q43900026 | ||
Plant pathogens trick guard cells into opening the gates | Q43993669 | ||
Dual fatty acyl modification determines the localization and plasma membrane targeting of CBL/CIPK Ca2+ signaling complexes in Arabidopsis. | Q44231298 | ||
A slow anion channel in guard cells, activating at large hyperpolarization, may be principal for stomatal closing | Q44544785 | ||
Arabidopsis NRT1.1 is a bidirectional transporter involved in root-to-shoot nitrate translocation. | Q45267985 | ||
Malate. Jack of all trades or master of a few? | Q45994221 | ||
Phospholipase Dδ is involved in nitric oxide-induced stomatal closure. | Q46040320 | ||
A molecular pathway for CO₂ response in Arabidopsis guard cells | Q46069941 | ||
Mechanisms and Physiological Roles of the CBL-CIPK Networking System in Arabidopsis thaliana | Q28069588 | ||
FLS2: an LRR receptor-like kinase involved in the perception of the bacterial elicitor flagellin in Arabidopsis | Q28141834 | ||
The MATE proteins as fundamental transporters of metabolic and xenobiotic organic cations | Q28265082 | ||
Abscisic acid activation of plasma membrane Ca(2+) channels in guard cells requires cytosolic NAD(P)H and is differentially disrupted upstream and downstream of reactive oxygen species production in abi1-1 and abi2-1 protein phosphatase 2C mutants | Q28363634 | ||
A possible CO2 conducting and concentrating mechanism in plant stomata SLAC1 channel | Q28477055 | ||
An abscisic acid-independent oxylipin pathway controls stomatal closure and immune defense in Arabidopsis | Q28488213 | ||
Mechanisms of abscisic acid-mediated control of stomatal aperture | Q28604202 | ||
FLS2 | Q29541156 | ||
Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair | Q30492418 | ||
Functional cloning and characterization of a plant efflux carrier for multidrug and heavy metal detoxification | Q30776706 | ||
SLAC1 is required for plant guard cell S-type anion channel function in stomatal signalling. | Q31147920 | ||
Abscisic acid induces oscillations in guard-cell cytosolic free calcium that involve phosphoinositide-specific phospholipase C. | Q31904146 | ||
CDPKs CPK6 and CPK3 function in ABA regulation of guard cell S-type anion- and Ca(2+)-permeable channels and stomatal closure | Q33259968 | ||
Plant nitrogen assimilation and its regulation: a complex puzzle with missing pieces | Q33360842 | ||
Regulation of sulfate assimilation in Arabidopsis and beyond | Q33579419 | ||
Abscisic acid-induced stomatal closure mediated by cyclic ADP-ribose | Q33617364 | ||
Control of vacuolar dynamics and regulation of stomatal aperture by tonoplast potassium uptake | Q33674493 | ||
Closing plant stomata requires a homolog of an aluminum-activated malate transporter. | Q33716847 | ||
Differential innate immune signalling via Ca(2+) sensor protein kinases | Q33739382 | ||
Guard cell anion channel SLAC1 is regulated by CDPK protein kinases with distinct Ca2+ affinities | Q33842779 | ||
Strong regulation of slow anion channels and abscisic acid signaling in guard cells by phosphorylation and dephosphorylation events. | Q33852204 | ||
Repetitive increases in cytosolic Ca2+ of guard cells by abscisic acid activation of nonselective Ca2+ permeable channels | Q33914943 | ||
Carbonic anhydrases are upstream regulators of CO2-controlled stomatal movements in guard cells | Q34003746 | ||
Membrane localization of a rice calcium-dependent protein kinase (CDPK) is mediated by myristoylation and palmitoylation | Q34103862 | ||
C(4) photosynthesis: principles of CO(2) concentration and prospects for its introduction into C(3) plants | Q34117702 | ||
Characterization of the NifS-like domain of ABA3 from Arabidopsis thaliana provides insight into the mechanism of molybdenum cofactor sulfuration | Q34370607 | ||
KAT1 is not essential for stomatal opening | Q34505334 | ||
Plant stomata function in innate immunity against bacterial invasion | Q34564415 | ||
A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence | Q34649229 | ||
Guard cell signal transduction network: advances in understanding abscisic acid, CO2, and Ca2+ signaling | Q34667667 | ||
AtALMT1, which encodes a malate transporter, is identified as one of several genes critical for aluminum tolerance in Arabidopsis | Q34687209 | ||
Identification of High-Affinity Slow Anion Channel Blockers and Evidence for Stomatal Regulation by Slow Anion Channels in Guard Cells. | Q46099873 | ||
The HT1 protein kinase is essential for red light-induced stomatal opening and genetically interacts with OST1 in red light and CO2 -induced stomatal movement responses | Q46300516 | ||
Dominant negative guard cell K+ channel mutants reduce inward-rectifying K+ currents and light-induced stomatal opening in arabidopsis | Q46307860 | ||
The ABC transporter AtABCB14 is a malate importer and modulates stomatal response to CO2. | Q46382806 | ||
MPK9 and MPK12 function in SA-induced stomatal closure in Arabidopsis thaliana | Q46388334 | ||
BRI1-Associated Receptor Kinase 1 Regulates Guard Cell ABA Signaling Mediated by Open Stomata 1 in Arabidopsis | Q46615889 | ||
Differential regulation of the expression of two high-affinity sulfate transporters, SULTR1.1 and SULTR1.2, in Arabidopsis. | Q46653931 | ||
Inactivation of PYR/PYL/RCAR ABA receptors by tyrosine nitration may enable rapid inhibition of ABA signaling by nitric oxide in plants. | Q46676067 | ||
The role of plasma membrane H(+) -ATPase in jasmonate-induced ion fluxes and stomatal closure in Arabidopsis thaliana | Q46713021 | ||
CO2 regulator SLAC1 and its homologues are essential for anion homeostasis in plant cells. | Q46729399 | ||
Two guard cell mitogen-activated protein kinases, MPK9 and MPK12, function in methyl jasmonate-induced stomatal closure in Arabidopsis thaliana | Q46769428 | ||
The regulatory domain of SRK2E/OST1/SnRK2.6 interacts with ABI1 and integrates abscisic acid (ABA) and osmotic stress signals controlling stomatal closure in Arabidopsis | Q46859360 | ||
ABA-induced NO generation and stomatal closure in Arabidopsis are dependent on H2O2 synthesis | Q46861018 | ||
Antisense repression reveals a crucial role of the plastidic 2-oxoglutarate/malate translocator DiT1 at the interface between carbon and nitrogen metabolism. | Q46861033 | ||
The Arabidopsis vacuolar malate channel is a member of the ALMT family. | Q46898719 | ||
The FLS2-associated kinase BIK1 directly phosphorylates the NADPH oxidase RbohD to control plant immunity. | Q46919321 | ||
Arabidopsis HT1 kinase controls stomatal movements in response to CO2. | Q46976396 | ||
Differential abscisic acid regulation of guard cell slow anion channels in Arabidopsis wild-type and abi1 and abi2 mutants | Q46976633 | ||
Guard cell inward K+ channel activity in arabidopsis involves expression of the twin channel subunits KAT1 and KAT2. | Q47820778 | ||
Malate- and pyruvate-dependent Fatty Acid synthesis in leucoplasts from developing castor endosperm | Q47917424 | ||
A family of putative chloride channels from Arabidopsis and functional complementation of a yeast strain with a CLC gene disruption | Q48056550 | ||
Expression of an Arabidopsis potassium channel gene in guard cells | Q48070455 | ||
Regulation of Stomatal Immunity by Interdependent Functions of a Pathogen-Responsive MPK3/MPK6 Cascade and Abscisic Acid | Q48170820 | ||
Unexpected protein families including cell defense components feature in the N-myristoylome of a higher eukaryote | Q48232874 | ||
A Single-Pore Residue Renders the Arabidopsis Root Anion Channel SLAH2 Highly Nitrate Selective | Q48300609 | ||
Ion Transport at the Vacuole during Stomatal Movements | Q48315668 | ||
Silent S-Type Anion Channel Subunit SLAH1 Gates SLAH3 Open for Chloride Root-to-Shoot Translocation | Q48546432 | ||
CHL1 functions as a nitrate sensor in plants. | Q48581674 | ||
C-terminus-mediated voltage gating of Arabidopsis guard cell anion channel QUAC1. | Q48632276 | ||
Switching between the two action modes of the dual-affinity nitrate transporter CHL1 by phosphorylation | Q34775427 | ||
Manipulating PEPC levels in plants | Q34785013 | ||
Nitric oxide negatively regulates abscisic acid signaling in guard cells by S-nitrosylation of OST1 | Q34985396 | ||
Phospholipase D alpha 1-derived phosphatidic acid interacts with ABI1 phosphatase 2C and regulates abscisic acid signaling | Q35322885 | ||
ABA activates multiple Ca(2+) fluxes in stomatal guard cells, triggering vacuolar K(+)(Rb(+)) release | Q35435796 | ||
The guard cell metabolome: functions in stomatal movement and global food security | Q35621171 | ||
THE ORGANIZATION AND REGULATION OF PLANT GLYCOLYSIS. | Q35687256 | ||
Ca2+ channels at the plasma membrane of stomatal guard cells are activated by hyperpolarization and abscisic acid. | Q35702023 | ||
Genome-wide identification of Calcineurin B-Like (CBL) gene family of plants reveals novel conserved motifs and evolutionary aspects in calcium signaling events | Q35738213 | ||
Plant sulphate transporters: co-ordination of uptake, intracellular and long-distance transport. | Q35838621 | ||
Calcium specificity signaling mechanisms in abscisic acid signal transduction in Arabidopsis guard cells | Q35866896 | ||
Two Arabidopsis guard cell-preferential MAPK genes, MPK9 and MPK12, function in biotic stress response | Q35932584 | ||
A protein phosphorylation/dephosphorylation network regulates a plant potassium channel. | Q36023781 | ||
Reconstitution of abscisic acid activation of SLAC1 anion channel by CPK6 and OST1 kinases and branched ABI1 PP2C phosphatase action | Q36068810 | ||
ClC chloride channels viewed through a transporter lens | Q36428974 | ||
Molecular Evolution of Slow and Quick Anion Channels (SLACs and QUACs/ALMTs). | Q36431618 | ||
Membrane voltage initiates Ca2+ waves and potentiates Ca2+ increases with abscisic acid in stomatal guard cells | Q36480637 | ||
Plant adaptation to fluctuating environment and biomass production are strongly dependent on guard cell potassium channels. | Q36516234 | ||
Guard cell ABA and CO2 signaling network updates and Ca2+ sensor priming hypothesis. | Q36607792 | ||
Light regulation of stomatal movement | Q36702122 | ||
Role of plant stomata in bacterial invasion. | Q36785882 | ||
AtALMT9 is a malate-activated vacuolar chloride channel required for stomatal opening in Arabidopsis | Q36815592 | ||
Arabidopsis nanodomain-delimited ABA signaling pathway regulates the anion channel SLAH3 | Q36855204 | ||
Two types of anion channel currents in guard cells with distinct voltage regulation | Q37040519 | ||
Nitric oxide, stomatal closure, and abiotic stress. | Q37106860 | ||
Review. CLC-mediated anion transport in plant cells. | Q37310613 | ||
MAP kinases MPK9 and MPK12 are preferentially expressed in guard cells and positively regulate ROS-mediated ABA signaling | Q37419503 | ||
Mechanisms of Cl(-) transport contributing to salt tolerance. | Q37628760 | ||
CLC transport proteins in plants | Q37663095 | ||
Two tonoplast MATE proteins function as turgor-regulating chloride channels in Arabidopsis | Q37695971 | ||
Anion channels/transporters in plants: from molecular bases to regulatory networks. | Q37833094 | ||
Regulation of the mitochondrial tricarboxylic acid cycle | Q38086704 | ||
The molybdenum cofactor | Q38094138 | ||
The role of K(+) channels in uptake and redistribution of potassium in the model plant Arabidopsis thaliana | Q38118757 | ||
A protein kinase, interacting with two calcineurin B-like proteins, regulates K+ transporter AKT1 in Arabidopsis. | Q50647480 | ||
PYR/RCAR receptors contribute to ozone-, reduced air humidity-, darkness-, and CO2-induced stomatal regulation. | Q50964059 | ||
The Arabidopsis calcium-dependent protein kinase, CPK6, functions as a positive regulator of methyl jasmonate signaling in guard cells. | Q52604670 | ||
N-myristoylation and S-acylation are common modifications of Ca2+ -regulated Arabidopsis kinases and are required for activation of the SLAC1 anion channel. | Q52677736 | ||
S-nitrosylation of NADPH oxidase regulates cell death in plant immunity. | Q52728434 | ||
Calcium-Dependent Protein Kinase CPK21 Functions in Abiotic Stress Response in Arabidopsis thaliana | Q52900780 | ||
Role of malate synthesis mediated by phosphoenolpyruvate carboxylase in guard cells in the regulation of stomatal movement. | Q53914423 | ||
Phosphorylation of the vacuolar anion exchanger AtCLCa is required for the stomatal response to abscisic acid. | Q54339356 | ||
The Calcineurin B-like calcium sensors CBL1 and CBL9 together with their interacting protein kinase CIPK26 regulate the Arabidopsis NADPH oxidase RBOHF. | Q54455805 | ||
The Arabidopsis GORK K+-channel is phosphorylated by calcium-dependent protein kinase 21 (CPK21), which in turn is activated by 14-3-3 proteins. | Q54983759 | ||
Multiple Calcium-Dependent Kinases Modulate ABA-Activated Guard Cell Anion Channels | Q56027359 | ||
CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease | Q56974848 | ||
The nitrate/proton antiporter AtCLCa mediates nitrate accumulation in plant vacuoles | Q59089752 | ||
Malate transport by the vacuolar AtALMT6 channel in guard cells is subject to multiple regulation | Q63443891 | ||
Plants have a sensitive perception system for the most conserved domain of bacterial flagellin | Q77908621 | ||
Nitric oxide-induced phosphatidic acid accumulation: a role for phospholipases C and D in stomatal closure | Q81584631 | ||
Involvement of extracellular oxidative burst in salicylic acid-induced stomatal closure in Arabidopsis | Q82378477 | ||
Release of Malate from Epidermal Strips during Stomatal Closure | Q83251938 | ||
Day-Night Variations in Malate Concentration, Osmotic Pressure, and Hydrostatic Pressure in Cereus validus | Q83260630 | ||
Danger-Associated Peptides Close Stomata by OST1-Independent Activation of Anion Channels in Guard Cells | Q88537336 | ||
A Tonoplast-Associated Calcium-Signaling Module Dampens ABA Signaling during Stomatal Movement | Q89093327 | ||
The mechanism of SO2 -induced stomatal closure differs from O3 and CO2 responses and is mediated by nonapoptotic cell death in guard cells | Q90266596 | ||
Guard Cell Salicylic Acid Signaling Is Integrated into Abscisic Acid Signaling via the Ca2+/CPK-Dependent Pathway | Q90424779 | ||
Transporters in plant sulfur metabolism | Q38253641 | ||
The roles of ROS and ABA in systemic acquired acclimation | Q38325620 | ||
Regulation of the NADPH Oxidase RBOHD During Plant Immunity. | Q38459105 | ||
Reactive Oxygen Species in the Regulation of Stomatal Movements | Q38840560 | ||
The varied functions of aluminium-activated malate transporters-much more than aluminium resistance | Q38860905 | ||
Sulfate availability affects ABA levels and germination response to ABA and salt stress in Arabidopsis thaliana. | Q38931267 | ||
Two calcineurin B-like calcium sensors, interacting with protein kinase CIPK23, regulate leaf transpiration and root potassium uptake in Arabidopsis. | Q38943283 | ||
Open or close the gate - stomata action under the control of phytohormones in drought stress conditions | Q38962688 | ||
Direct regulation of the NADPH oxidase RBOHD by the PRR-associated kinase BIK1 during plant immunity | Q39015503 | ||
Stomatal closure by fast abscisic acid signaling is mediated by the guard cell anion channel SLAH3 and the receptor RCAR1. | Q39020008 | ||
The nitrate transporter AtNRT1.1 (CHL1) functions in stomatal opening and contributes to drought susceptibility in Arabidopsis. | Q39036806 | ||
A plasma membrane receptor kinase, GHR1, mediates abscisic acid- and hydrogen peroxide-regulated stomatal movement in Arabidopsis | Q39083185 | ||
Chloride on the Move | Q39084248 | ||
Open stomata 1 (OST1) kinase controls R-type anion channel QUAC1 in Arabidopsis guard cells | Q39093881 | ||
Regulation of abscisic acid-induced stomatal closure and anion channels by guard cell AAPK kinase | Q39175689 | ||
AtCPK23 functions in Arabidopsis responses to drought and salt stresses | Q39198201 | ||
Site- and kinase-specific phosphorylation-mediated activation of SLAC1, a guard cell anion channel stimulated by abscisic acid. | Q39205784 | ||
Drought-Enhanced Xylem Sap Sulfate Closes Stomata by Affecting ALMT12 and Guard Cell ABA Synthesis | Q39207575 | ||
AtALMT12 represents an R-type anion channel required for stomatal movement in Arabidopsis guard cells | Q39248489 | ||
Arabidopsis OST1 protein kinase mediates the regulation of stomatal aperture by abscisic acid and acts upstream of reactive oxygen species production | Q39284356 | ||
Disruption of the Arabidopsis thaliana inward-rectifier K+ channel AKT1 improves plant responses to water stress. | Q39304410 | ||
Stomatal Defense a Decade Later. | Q39305071 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | guard cell | Q241368 |
SALT STRESS | Q57671505 | ||
Drought Stress | Q59944593 | ||
P304 | page(s) | 9 | |
P577 | publication date | 2019-01-03 | |
P1433 | published in | Plants | Q27724544 |
P1476 | title | Guard Cell Membrane Anion Transport Systems and Their Regulatory Components: An Elaborate Mechanism Controlling Stress-Induced Stomatal Closure | |
P478 | volume | 8 |
Q98735656 | Barley ABI5 (Abscisic Acid INSENSITIVE 5) Is Involved in Abscisic Acid-Dependent Drought Response |
Q89965990 | Calcium-Regulated Phosphorylation Systems Controlling Uptake and Balance of Plant Nutrients |
Q90224320 | Chloride as a Beneficial Macronutrient in Higher Plants: New Roles and Regulation |
Q92539294 | Coping With Water Shortage: An Update on the Role of K+, Cl-, and Water Membrane Transport Mechanisms on Drought Resistance |
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